Medical Device Recalls
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1 result found
510(K) Number: K790108 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid an... | 2 | 06/07/2018 | CareFusion 303, Inc. |
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